Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604558Generated: November 2, 2026

Triphenylphosphine → (1-Ethylpyrrol-2-yl)methyltriphenylphosphonium iodide

https://huagongshe.com/reaction/604558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(1-Ethylpyrrol-2-yl)methyltrimethylammonium iodideHCID 23031652—
SolventAcetonitrileHCID 6342—
Product(1-Ethylpyrrol-2-yl)methyltriphenylphosphonium iodideHCID 2303150281.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

(1-Ethylpyrrol-2-yl)methyltrimethylammonium iodide (20.0 g, 68.0 mmol) was suspended in acetonitrile (200 mL) and triphenylphosphine (22.0 g, 83.9 mmol) was added thereto, followed by stirring of the mixture at 80° C. for 9 hours. After cooling, the mixture was concentrated to about ½ under reduced pressure and ethyl acetate (100 mL) was added thereto. The precipitated crystal was collected by filtration, washed with ethyl acetate and dried under reduced pressure to obtain the title compound (27.5 g, yield: 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910617B2
Source datasetuspto-grants-2011_03
ORD IDord-e283bf67d68a492ea769b0c54cf146cf
Source noteuspto-grants-2011_03